HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993816Generated: October 26, 2026
Hydrochloric Acid → 2-Cyano-2-(3-phenoxy-phenylthiocarbamoyl)-acetamide
https://huagongshe.com/reaction/1993816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Phenoxyphenylisothiocyanate | HCID 22041281 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyano-2-(3-phenoxy-phenylthiocarbamoyl)-acetamide | HCID 86607393 | 72.4% |
Reaction Steps
To a suspension of 85% powdered KOH in 20 ml DMF was added 1.74 g of cyanoacetamide at room temperature. The solution was stirred at room temperature for 15 minutes and then cooled in a water bath at room temperature. To this solution 4.7 g of 3-phenoxy-phenyl isothiocyanate was added dropwise. The solution exothermed slightly with the internal temperature rising to 28° C. during the addition. The solution was stirred at room temperature for 16 h, then diluted with 150 ml water and extracted with ethyl acetate to remove small amounts of starting material and by-products. The aqueous layer was isolated and acidified with 1N HCl to pH 1 with vigorous stirring. The resulting tan precipitate was filtered, washed with water, and dried for 16 hours in a vacuum oven to afford 4.66 g of 2-cyano-2-(3-phenoxy-phenylthiocarbamoyl)-acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652047B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-21667798801a4c99b11a35f3cad41684 |
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| Source note | uspto-grants-2010_01 |
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